Search

This article provides detailed redox data on nine differently substituted benzophenones and ten square planar copper(II) complexes containing 2-hydroxyphenones obtained by cyclic voltammetry (CV) experiments. The information provided is related to the published full research articles “An electrochemical and computational chemistry study of substituted benzophenones” (Electrochim. Acta2021, 373, 137894) and “Electrochemical behaviour of copper(II) complexes containing 2-hydroxyphenones” (Electrochim. Acta2022, 424, 140629), where the CVs and electrochemical data at mainly one scan rate, namely at 0.100 Vs−1, are reported. CVs and the related peak current and voltage values, not reported in the related research article, are provided in this article for nine differently substituted benzophenones and ten differently substituted copper-2-hydroxyphenone complexes at various scan rates over more than two orders of magnitude. The redox data presented are the first reported complete set of electrochemical data of nine 2-hydroxyphenones and ten copper(II) complexes containing 2-hydroxyphenone ligands.

Theoretical investigations by density functional theory (DFT) and time-dependent DFT (TD-DFT) methods shed light on how the type of ligand or attached groups influence the electronic structure, absorption spectrum, electron excitation, and intramolecular and interfacial electron transfer of the Cu(II) complexes under study. The findings provide new insight into the designing and screening of high-performance dyes for dye-sensitized solar cells (DSSCs).

Metal organic frameworks (MOFs) are porous hybrid crystalline materials that consist of organic linkers coordinated to metal centres. The trans–cis isomerisation kinetics of the azobenzene-4,4′-dicarboxylic acid (AZB(COOH)2) precursor, as well as the Al3+ (Al-AZB)- and Zr4+ (Zr-AZB)-based MOFs with azobenzene-4,4′-dicarboxylate linkers, are presented. The photo-isomerization in the MOFs originates from singly bound azobenzene moieties on the surface of the MOF. The type of solvent used had a slight effect on the rate of isomerization and half-life, while the band gap energies were not significantly affected by the solvents. Photo-responsive MOFs can be classified as smart materials with possible applications in sensing, drug delivery, magnetism, and molecular recognition. In this study, the MOFs were applied in the dye adsorption of congo red (CR) in contaminated water. For both MOFs, the UV-irradiated cis isomer exhibited a slightly higher CR uptake than the ambient-light exposed trans isomer. Al-AZB displayed a dye adsorption capacity of over 95% for both the UV-irradiated and ambient light samples. The ambient light exposed Zr-AZB, and the UV irradiated Zr-AZB had 39.1% and 44.6% dye removal, respectively.